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PubMed:19365571 / 0-173 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-84 Sentence denotes Macular corneal dystrophy in a Chinese family related with novel mutations of CHST6.
T2 85-93 Sentence denotes PURPOSE:

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
5968 0-25 DiseaseOrPhenotypicFeature denotes Macular corneal dystrophy MESH:D003317
5969 78-83 GeneOrGeneProduct denotes CHST6 NCBIGene:4166
5970 123-157 GeneOrGeneProduct denotes carbohydrate sulfotransferase gene NCBIGene:4166
5971 159-164 GeneOrGeneProduct denotes CHST6 NCBIGene:4166

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 0-25 DiseaseOrPhenotypicFeature denotes Macular corneal dystrophy 0009020
T2 8-25 DiseaseOrPhenotypicFeature denotes corneal dystrophy 0018102

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 26-30 GeneOrGeneProduct denotes in a
T2 59-64 GeneOrGeneProduct denotes novel
T3 65-74 GeneOrGeneProduct denotes mutations
T4 78-83 GeneOrGeneProduct denotes CHST6
T5 106-115 GeneOrGeneProduct denotes mutations
T6 123-152 GeneOrGeneProduct denotes carbohydrate sulfotransferase
T7 159-164 GeneOrGeneProduct denotes CHST6

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 59-64 GeneOrGeneProduct denotes novel
T2 78-83 GeneOrGeneProduct denotes CHST6
T3 123-152 GeneOrGeneProduct denotes carbohydrate sulfotransferase
T4 159-164 GeneOrGeneProduct denotes CHST6

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 8-25 DiseaseOrPhenotypicFeature denotes corneal dystrophy D003317

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 78-83 GeneOrGeneProduct denotes CHST6
T2 123-152 GeneOrGeneProduct denotes carbohydrate sulfotransferase
T3 159-164 GeneOrGeneProduct denotes CHST6

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 0-25 DiseaseOrPhenotypicFeature denotes Macular corneal dystrophy 0009020

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 8-25 DiseaseOrPhenotypicFeature denotes corneal dystrophy D003317

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 8-25 DiseaseOrPhenotypicFeature denotes corneal dystrophy D003317

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 123-152 ChemicalEntity denotes carbohydrate sulfotransferase C118929

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T1 123-152 ChemicalEntity denotes carbohydrate sulfotransferase C118929
T3 159-164 GeneOrGeneProduct denotes CHST6
T69046 123-152 GeneOrGeneProduct denotes carbohydrate sulfotransferase
T96841 78-83 GeneOrGeneProduct denotes CHST6
T78325 8-25 DiseaseOrPhenotypicFeature denotes corneal dystrophy D003317

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 0-25 DiseaseOrPhenotypicFeature denotes Macular corneal dystrophy 0009020

DisGeNET

Id Subject Object Predicate Lexical cue
T0 159-164 gene:4166 denotes CHST6
T2 159-164 gene:4166 denotes CHST6
T4 159-164 gene:4166 denotes CHST6

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
19365571-1#65#70#gene4166 159-164 gene4166 denotes CHST6